ライフサイエンスコーパス: polychaete

1 bundant birds, fishes, burrowing shrimps and polychaetes.

2 ro-dimer formation in the GKs from these two polychaetes.

3 loss from animal tissues were 20% d(-1) for polychaetes, 10% d(-1) for crabs, and 6% d(-1) for fish

4 We estimate that up to 18,500 ornamental polychaetes (16,980 sabellids and 1,018 serpulids) are s

5 The Hb from the deep-sea polychaete Alvinella exhibited in addition, peaks at app

6 Dehaloperoxidase (DHP) from the terebellid polychaete Amphitrite ornata is a bifunctional enzyme th

7 Dehaloperoxidase (DHP) from the terebellid polychaete Amphitrite ornata is a bifunctional enzyme th

8 dehaloperoxidase (DHP), from the terebellid polychaete Amphitrite ornata is designed to catalyze the

9 The terebellid polychaete Amphitrite ornata produces no detectable vola

10 (DHP), found in the coelom of the terebellid polychaete Amphitrite ornata, is a dual-function protein

11 gen transport hemoglobin from the terebellid polychaete Amphitrite ornata, is the first globin identi

12 e (DHP), discovered in the marine terebellid polychaete Amphitrite ornata, is the first heme-containi

13 al function protein found in the terrebellid polychaete Amphitrite ornata.

14 (Hb) originally isolated from the terebellid polychaete Amphitrite ornata.

15 rect contribution of two macrofaunal groups, polychaetes and bivalves, to methane and nitrous oxide f

16 ssemblages differed, with significantly less polychaetes and more oligochaetes in treatments exposed

17 ylsiloxane (PDMS), and organisms ranged from polychaetes and oligochaetes to bivalves, aquatic insect

18 solated mineral-free exception (e.g., marine polychaetes and squids), minerals are thought to be indi

19 The Annelida, which includes the polychaetes and the clitellates, has long held the taxon

20 shima sediment, up to 55% in crabs ingesting polychaetes, and about 80% in fish ingesting worms.

21 sufficiently bioavailable to deposit-feeding polychaetes, and macrofauna assimilate Cs from these pol

22 However, unlike the case found in polychaete annelid and soil nematode embryos, there is n

23 g/Wnt1) in larval and juvenile stages of the polychaete annelid Capitella sp. I and en in a second po

24 uring larval and juvenile development in the polychaete annelid Capitella sp. I., a member of the thi

25 x genes in embryos of a lophotrochozoan, the polychaete annelid Chaetopterus sp.

26 In the equally cleaving embryo of the polychaete annelid Hydroides, MAPK activation was not de

27 d along the proximodistal axis of developing polychaete annelid parapodia, onychophoran lobopodia, as

28 u hybridization in larvae of Chaetopterus, a polychaete annelid with a tagmatized axial body plan.

29 interpreted as a primitive mollusc and as a polychaete annelid worm.

30 Polychaete annelids and arthropods are both segmented pr

31 erns which suggest that both sea urchins and polychaete annelids use Hox genes in a very similar fash

32 e arthropods and the nonganglionic brains of polychaete annelids, polyclad planarians, and nemerteans

33 Polychaetes are frequented in toxicological studies, one

34 esponses in early life history stages of the polychaete Arenicola marina and found both synergistic a

35 provides the first assessment of ornamental polychaetes but more importantly highlights the issues s

36 Part of this rich diversity includes annelid polychaetes but unfortunately, our understanding of such

37 f a segmentation gene homologue in the basal polychaete Capitella capitata using a pan-annelid cross-

38 holine-binding protein (AChBP) in the marine polychaete Capitella teleta, from the annelid phylum.

39 creatine kinase (CK) from a protostome, the polychaete Chaetopterus variopedatus, were elucidated an

40 gene engrailed (en) in a basal annelid, the polychaete Chaetopterus.

41 were 45% d(-1), 14% d(-1), and 5% d(-1) for polychaetes, crabs, and fish, respectively.

42 similar to each other than to microbiomes of polychaetes, decapods and fish.

43 hey display many characteristics atypical of polychaete eyes, such as ciliary photoreceptors [3,4] th

44 eatures seen in several different Palaeozoic polychaete families.

45 r and possessed the largest jaws recorded in polychaetes from the fossil record, with maxillae reachi

46 in and it has been compared with nemerteans, polychaetes, gastropods, conodonts, and the stem arthrop

47 This demonstrates that polychaete gigantism was already a phenomenon in the Pal

48 A re-description of the polychaete groups traded using a combination of molecula

49 The polychaete Hox complex is shown not to be expressed duri

50 Larvae of the serpulid polychaete Hydroides elegans can be induced to settle by

51 he molecular mechanism suggested for another polychaete, Hydroides elegans, highlighting likely molec

52 e annelid Capitella sp. I and en in a second polychaete, Hydroides elegans.

53 ehaloperoxidase activities in other infaunal polychaetes, including halometabolite-producing species.

54 Polychaetes indirectly enhance methane efflux through bi

55 ssimilation efficiency of (137)Cs was 16% in polychaetes ingesting Fukushima sediment, up to 55% in c

56 In the polychaete jaws, HIS-rich sequences are expanded into a

57 n two noncellular tissues, mussel byssus and polychaete jaws, recent studies suggest that one natural

58 E1 is longer and E2 is shorter in the polychaete MiCK gene than the counterpart sarcomeric and

59 lopsis oscura and the chlorocruorin from the polychaete Myxicola infundibulum, over the pH range 3.5-

60 Prior work has shown that GK from the polychaete Neanthes (Nereis) diversicolor exits as a het

61 ly with tissue residue in the marine benthic polychaete Neanthes arenaceodentata exposed in the same

62 We have been studying one population of the polychaete Nereis (Hediste) diversicolor exhibiting inhe

63 which is released by swimming females of the polychaete Nereis succinea to activate spawning behavior

64 was significantly accumulated in the marine polychaete Nereis virens (N. virens) in the AgNP-citrate

65 In contrast with vertebrate MiCK, polychaete octamers are very stable indicating that dime

66 s are found at hydrothermal vents, where the polychaete Paralvinella sulfincola lives on vent sulfide

67 Acid-tolerant polychaetes (Polynoidae) live in this environment, appar

68 mber and provenance of species of ornamental polychaetes (sabellids and serpulids) traded was underta

69 and molecular analyses show that two further polychaete species are shared with vents beyond the Indi

70 time of AP pattern formation in leech and in polychaete suggests that the anterior organizing functio

71 worm, Sabellaria alveolata, a reef-building polychaete that supports high biodiversity, we carried o

72 , which inhabits estuary mudflats with other polychaetes that secrete a range of toxic brominated phe

73 Fan worms (Annelida: Sabellidae) are sessile polychaetes that spend their adult lives in tubes and pr

74 low oxygen levels on the feeding ecology of polychaetes, the dominant macrofaunal animals in deep-se

75 tes, and macrofauna assimilate Cs from these polychaetes to account for >90% of their body burden.

76 umbricus terrestris and Tubifex tubifex, the polychaetes Tylorrhynchus heterochaetus, Arenicola marin

77 nd I provide examples for insects, molluscs, polychaetes, vertebrates and flowering plants.

78 Here we describe a new eunicidan polychaete, Websteroprion armstrongi gen.

79 These polychaetes were thermotaxic, preferring temperatures of

80 High copper levels in the polychaete worm Glycera dibranchiata recently were attri

81 ette filter toxicants and microfibres on the polychaete worm Hediste diversicolor (ragworm), a widesp

82 Inspired by the polychaete worm jaw, we report a novel approach to gener

83 of zinc also occur in the jaws of the marine polychaete worm Nereis sp.

84 the dominance and distribution of the known polychaete worm species living in a naturally acidic sea

85 on metals zinc and copper in the jaws of two polychaete worm species Nereis and Glycera, respectively

86 The vent-associated polychaete worm, Alvinella pompejana, is host to a visib

87 n vent ecosystems in other oceans, including polychaete worms (Siboglinidae), bathymodiolid mussels,

88 Whilst the fossil record of polychaete worms extends to the early Cambrian, much dat

89 ct undamaged cryptic respiring prey, such as polychaete worms.